FDA GFI, Testing of Glycerin, Propylene Glycol, Maltitol, and other High-Risk Drug Components for Diethylene Glycol and Ethylene Glycol, 05/23 Anastasija Eschricht2023-06-14T11:04:43+00:00June 14th, 2023|
EMA Questions and Answers: API as starting material in Veterinary medicinal products, 02/22 Anastasija Eschricht2023-06-09T11:30:04+00:00March 21st, 2023|
EMA Question and Answers: Active substance registration, 07/18 Anastasija Eschricht2023-03-21T12:46:43+00:00March 21st, 2023|
EMA Questions and Answers: GMP Guide Part II API Anastasija Eschricht2023-03-16T14:17:46+00:00March 16th, 2023|
ICH Guideline Continuous Manufacturing of Drug Substances and Drug Products Q13, 11/22 Anastasija Eschricht2023-02-24T09:11:24+00:00February 24th, 2023|
EMA Guideline Excipients in the dossier for application for marketing authorisation of a medicinal product, 06/07 Anastasija Eschricht2022-12-07T10:14:15+00:00December 7th, 2022|